Ganesh Adluru1, Edward V R Dibella. 1. Laboratory for Structural NMR Imaging, Department of Radiology, University of Pennsylvania, Philadelphia, PA 19104, USA.
Abstract
Recently, there has been a significant interest in applying reconstruction techniques, like constrained reconstruction or compressed sampling methods, to undersampled k-space data in MRI. Here, we propose a novel reordering technique to improve these types of reconstruction methods. In this technique, the intensities of the signal estimate are reordered according to a preprocessing step when applying the constraints on the estimated solution within the iterative reconstruction. The ordering of the intensities is such that it makes the original artifact-free signal monotonic and thus minimizes the finite differences norm if the correct image is estimated; this ordering can be estimated based on the undersampled measured data. Theory and example applications of the method for accelerating myocardial perfusion imaging with respiratory motion and brain diffusion tensor imaging are presented.
Recently, there has been a significant interest in applying reconstruction techniques, like constrained reconstruction or compressed sampling methods, to undersampled k-space data in MRI. Here, we propose a novel reordering technique to improve these types of reconstruction methods. In this technique, the intensities of the signal estimate are reordered according to a preprocessing step when applying the constraints on the estimated solution within the iterative reconstruction. The ordering of the intensities is such that it makes the original artifact-free signal monotonic and thus minimizes the finite differences norm if the correct image is estimated; this ordering can be estimated based on the undersampled measured data. Theory and example applications of the method for accelerating myocardial perfusion imaging with respiratory motion and brain diffusion tensor imaging are presented.
There
has been large interest in speeding the acquisition of MRI data by acquiring
fewer samples in k-space and resolving the artifacts. Recently, there have been
significant advances in applying inverse problem techniques to
reconstruct images from undersampled k-space MRI data [1-6]. The methods use nonuniform undersampling and
a nonlinear recovery scheme in which a constraint, such as a spatial total
variation (TV) constraint [7], is applied on the estimated solution, while preserving
fidelity to the acquired data in k-space. It has been shown [2] that using an L
1
norm or a TV norm as constraint exploits the implicit sparsity in the data, and
can be used in both space and time dimensions. The method is best known to
reconstruct piecewise constant or smoothly varying data from its undersampled
Fourier samples; but the application of the method to MR imaging techniques
like dynamic contrast enhanced myocardial perfusion imaging (with respiratory
motion in the data) and diffusion tensor imaging (DTI) can be limited as these
images are often not piecewise constant.In
this paper, we propose a technique to improve the reconstruction of
general signals that may not fit the TV constraint well. The technique uses
preprocessing of the measured undersampled data to determine an improved
ordering of the pixel intensities of the image estimate. If an ordering that
improves the match of the estimated images and the constraint being used within
the reconstruction can be
found, an improved reconstruction can result. The image estimates are
reordered solely to be used with the constraint or regularization term in the
iterative reconstruction. The reordering approach is general in its
applicability and can be used in contexts which are based on regularization
techniques and in which ordering of the image intensities can be determined a priori. In the next sections, we
give a brief overview of the compressed sampling or constrained reconstruction
method for MRI from a regularization point of view and then present the theory
and applications of the reordering method.
The
compressed sampling method is described rigorously from a mathematical
standpoint recently in a series of papers [2, 8–10]. The method
is used to reconstruct a signal from a set of random Fourier samples below the
Nyquist rate by solving a convex optimization problem, in which fidelity to the
measured data is preserved at sample locations, while applying an L
1
or a TV constraint on the estimated solution. The method exploits the implicit
sparsity in the estimated solution or a transform of the estimated solution.
One useful transform for signals or images is finite differences as the signals
that are not directly sparse can be sparse in terms of finite differences
(especially piecewise constant or smoothly varying signals or images) and hence
an L
1
norm of finite differences (TV norm) is used.Although
the L
1 norm of the signal or image estimate is not a direct measure
of sparsity in the data, it has been shown that for a wide variety of data
using an L
1 norm is equivalent to using the L
0
norm (the
number of nonzero samples), which is a direct measure of sparsity [2]. Solving
the optimization problem with an L
1
norm is generally easier than
solving the problem with an L
0
norm.The
compressed sampling method when applied to MR image reconstruction can be
thought as a constrained reconstruction method in an inverse problem framework
[3, 11–14]. For the 1D case, the relation between Fourier data and the signal
space estimate can be represented as F
m = d, where m is the signal of interest, d is the
fully sampled k-space data, and F represents the Fourier transform; but it often takes a long time to acquire
full k-space data and results in tradeoffs in image quality, resolution, and
coverage of the organ. To accelerate the data acquisitions, when full data are
not acquired in k-space, and only undersampled data are acquired, the relation
between the artifact-free signal estimate and acquired data is given by where W implements a binary undersampling pattern with ones (where data are
acquired) and zeros (where data are missing), and is the undersampled Fourier data.
Reconstructing the signal directly using (1) is not feasible as W
−1 does not exist in general and hence
the solution is not unique.Regularization
techniques can be used to solve this ill-posed problem. The existence of the
solution is imposed by considering least-square solutions which minimize the functional ,
where ||·||2 represents an L
2
norm. Uniqueness
of the solution is imposed by using one or more constraints on the solution. A
popular constraint used in the field of compressed sampling is the total
variation constraint given by ,
where ∇ is the gradient of the estimated signal, ε is a small positive constant to avoid
singularities in the derivative of the functional [15], and ||·||1 represents an L
1
norm.Reconstruction
is performed by minimizing a convex cost function (C) Hence, a
solution which preserves fidelity to the acquired data and which has the
minimum total variation is chosen as the final solution. In (2), α is the regularization parameter which controls
the tradeoff between the fidelity and the constraint terms. The total variation
constraint helps to resolve the artifacts while not penalizing the edges
heavily.The
method can be extended to 2D and multi-image dimensions and it works very well
when the k-space data are undersampled in an irregular fashion and the
underlying complex images are smoothly varying or are piecewise constant [2].
When the images are not piecewise constant (which is the case for most MR
images), the performance of the method can be affected. We describe below a
reordering method to improve the performance of the constrained reconstruction
method when the data do not match the constraints well. The method preprocesses
the signal to select a monotonic ordering of the estimated solution in space
and/or time and incorporates the reordering in the constraints to obtain better
reconstructions.For
clarity, the reordering method is first described for the 1D case and then the
method is extended to 2D and multidimension cases. Applications of the
reconstruction method with reordering for dynamic myocardial perfusion imaging
with respiratory motion and for brain DTI data are presented.
2.2. Reordering method: 1D case
When
the signal of interest is varying rapidly and is not smooth or the data are not
piecewise constant, the total variation of the signal is already high and hence
reconstruction from undersampled Fourier domain samples can be inaccurate.
Consider, for example, a smoothly varying 1D signal and a rapidly varying
signal that are labeled “original full data” as shown in Figures 1(a) and 1(b), respectively. When the corresponding Fourier samples (k-space data) of
the curves are undersampled by a factor of two in a pseudorandom fashion (using
“rand” function in MATLAB (The Mathworks, Natick, Mass, USA)) and
reconstructed using the inverse Fourier transform, the signals labeled “undersampled
data R = 2” in Figures 1(a) and 1(b) are obtained. When these undersampled
signals are reconstructed according to (2), the curves in Figures 1(c) and 1(d)
are obtained. The original curves are overlaid in Figures 1(c) and 1(d) for
reference.
Figure 1
(a) A fully sampled smoothly varying 1D signal and the corresponding
signal reconstructed using IFT from its incomplete Fourier data undersampled by
a factor of two (R~2) in a random fashion. (b) A fully sampled nonsmooth varying 1D signal and the corresponding signal
reconstructed using IFT from its R~2 Fourier data undersampled in a random
fashion. (c) Comparison of the
original fully sampled smooth signal and the reconstructed signal from R~2
Fourier data without reordering. (d) Comparison of the original fully sampled nonsmooth signal and the corresponding
signal reconstructed from R~2 Fourier data without reordering. (e) Comparison of the original fully
sampled nonsmooth signal and the corresponding sorted signal. (f) Comparison of the original fully
sampled nonsmooth signal and the signal reconstructed from R~2 Fourier data
with reordering.
Reconstruction
using (2) is better for the smooth curve in Figure 1 as compared to that for
the rapidly varying curve. To improve the reconstruction in the latter case, we
first reorder the estimated curve in the signal space according to an optimal
order, and then apply the total variation constraint. The optimal ordering can
be determined as the ordering that makes the signal intensities in the curve
from the fully sampled dataset monotonic and smoothly varying. Reordering the
estimated solution helps by reducing sudden variations in the curves and gives
a better match to the assumed constraint. In practice, the curve or images from
fully sampled data will not be available to obtain the optimal ordering and
some sort of approximate reconstruction must be used to determine the ordering.
While this area needs more research, we show here that relatively simple
methods for determining reorderings can improve reconstructions of some types
of undersampled data.Better
reconstruction from the undersampled Fourier samples is obtained when the
reordered curve is used in the constraint term, as the a priori assumption that the curve has lower variation is better
satisfied. So the new reconstruction from undersampled data is performed
according to (3) in which the only difference is that the TV constraint is
applied on the reordered data as opposed to applying the constraint directly on
the given data. Reordering the estimated signal can also be thought as
multiplication of the signal with a reordering matrix “P.” This matrix can be a permutation matrix of ones and zeros (it
could also be a diagonal matrix for a 1D signal and it can be generalized for
multidimensional signals) as follows:Note
that the reordering in (3) is not directly based on the intensity values
obtained from the aliased signal from undersampled data in k-space (or for
other applications, whatever domain the measurement data is obtained). That is, P is determined once, and is fixed
while minimizing (3). Ordering the undersampled data according to the optimal
order does not mean that the reordered undersampled image estimates are
monotonic, but means that
if this ordering is used, the original full data in the signal space will best
match the TV constraint. Consider Figure 1(e) which shows the sorted curve of
the original curve in Figure 1(b). The curve is monotonic and smoothly varying
and has lower total variation as compared to the original curve.The
reconstruction obtained with reordering is shown in Figure 1(f). The ordering
in this case was chosen as the sorting order that made the original full curve
monotonic and smoothly varying. The reconstructed and the original signals
match very closely. Although not shown
here, the reconstruction with reordering was comparable to that without
reordering for the case of the smooth curve in Figure 1(a).From
the compressed sampling point of view, reordering the data can lead to sparser
representations of the data and hence higher acceleration factors.
Alternatively, better reconstructions for a given acceleration factor can be
obtained. Figure 2 illustrates the point for the original full curve shown in
Figure 1(b). The figure compares the sparsity of the original curve and the
sorted curve in terms of finite differences. The finite difference curve for
the sorted signal is sparser (has fewer nonzero values) as compared to that of the
original signal and hence using an L
1
norm of the finite differences
with reordering leads to better reconstructions.
Figure 2
Comparison of sparsity of the
fully sampled original nonsmooth signal in Figure 1(b) and that of the
corresponding sorted signal in terms of finite differences.
2.3. Choice of the regularization parameter, α
Choosing
the optimal regularization parameter
α
is important to obtain good
reconstructions. The L-curve method [16] is a popular technique for choosing
the optimal value. The method can be used when reordering is used. The fidelity
norm is plotted against the constraint norm of the reordered data and the optimal
parameter is given by the corner of the L-curve. Figures 3(a) and 3(b) show the
L-curves obtained for reconstructions from undersampled data for the curve
shown in Figure 1(b) without and with reordering, respectively. The L-curve in
Figure 3(a) is also overlaid on Figure 3(b) for direct comparison. The L-curves
and the optimal parameters obtained are different for both cases. The optimal
parameter without reordering is higher than that with reordering. As in the iterative methods, the number of
iterations also plays the role of regularization parameter; a fixed maximum
number of iterations which gave minimum RMS reconstruction error for various
α
values was chosen in computing the L-curves.
Figure 3
Comparison of optimal
regularization weights without and with reordering. L-curves obtained for reconstruction of the
nonsmooth signal in Figure 1(b) from R~2 Fourier data (a) without reordering and (b) with reordering overlaid by the L-curve in Figure 3(a).
2.4. Inaccurate reordering
From
the above, it is apparent that correct reordering can help in better
reconstruction from undersampled Fourier data when the signals are not smoothly
varying. In the above experiment, we used full data to determine the optimal
ordering. To be able to use the
reordering method, we need to have an ordering that makes the original signal best
match the constraint. In practice, it is likely not possible to get the exact
ordering of the signal curves or images as that obtained using fully sampled
Fourier data due to various factors like blurring of the prior signal, noise in
the prior signal, and so on. To simulate this case, we randomly perturbed the
exact sorting order to see the effect of having inexact ordering on the
performance of the algorithm.In Figure 4, the
X-axis represents the number of random perturbations, that is, the number of indices of
the exact “sorting-order vector” that are randomly perturbed. Consider S to be the sorting-order vector for the original signal. When there is one
random perturbation, (i) a random number is generated between 1 and the length
of S denoted by r_a, then (ii) a second distinct random number between 1 and the
length of S denoted by r_b, and finally (iii) the value of the S at index r_a is exchanged with that at index r_b. A value of 10 on the X-axis means that the
values of the exact “sorting-order vector” at 10 distinct randomly picked
indices (out of 70) are exchanged with those at a different set of 10 distinct
randomly picked indices. The Y-axis represents the natural log of the total
absolute difference between original full data and the reconstructed signal. We
can see that as the number of random perturbations increases, the total absolute error
using reordering gradually increases, but this number is still better or comparable to that
without the reordering except for a few perturbations toward the end of the
plot where the entire sorting-order vector was randomly perturbed.
Figure 4
Comparison of errors in the
reconstruction for the nonsmooth signal in Figure 1(b) without reordering and
with reordering as a function of inaccuracies in the ordering.
2.5. Reconstruction with reordering: 2D case
The
reordering method described above for the 1D case can be extended to 2D and
applied in the context of images. As in the 1D case, reordering in 2D for
images helps in better reconstruction when the images of interest are nonsmooth
or are not piecewise constant. For
example, Figure 5(a) shows a simulated piecewise constant heart image with
blood pools and with an ischemic region in the myocardium. When full Fourier
data of the image are undersampled in a variable density (VD) Cartesian fashion
[5] (so that 5 lines in the center of k-space are fully sampled and the
remaining phase encodes are sampled in a pseudorandom fashion to give a net
reduction factor of ~6.5), direct inverse Fourier transform reconstruction
gives the image shown in Figure 5(b). When the constrained reconstruction
approach with a TV spatial constraint () without reordering is used, Figure 5(c) is
obtained. We can see that Figure 5(c) matches well with Figure 5(a); but when the
image is not piecewise constant, the performance of the constrained
reconstruction can be affected. Figure 5(d) shows an actual MR heart image from
a patient at a single time in a perfusion sequence. The image was reconstructed
using a standard 2D inverse Fourier transform of the fully acquired k-space
data. Figure 5(e) shows the standard 2D inverse Fourier transform
reconstruction of undersampled k-space data for the time frame, with zeros
inserted for the missing k-space data points. The data were undersampled by a factor of three in
VD Cartesian fashion (10 phase encodes fully sampled around the center and the
remaining ones in a pseudorandom fashion). Figure 5(f)
shows the constrained reconstruction from the undersampled data using a spatial
TV constraint without any reordering which has a few residual artifacts. For
improving the reconstruction in this case, the image is reordered independently
in x and y directions before applying the 2D TV constraint, that is, reorderings
are determined separately for each row and each column. In practice, since the
data we deal with in MRI are
complex, the optimal ordering is determined independently for the real and
imaginary components of the image and separately in x and y directions. A row-reordered real part
of the image of the original complex
MR image of the heart is shown in Figure 5(g). The TV spatial constraint with
reorderings for a complex image can be explicitly written as , where , in which is the real part of the image estimate and is the imaginary part of the image
estimate. P and P denote the reordering matrices for ordering the signal in x dimension for the real and imaginary parts, respectively, while P and P are the corresponding reordering matrices in y dimension. For simplicity and
compactness, the above spatial constraint with reordering is referred to as where gives the image reordered for each row in the x direction and is the image reordered for each column in the y direction. Figure 5(h) shows the
reconstruction from the undersampled data using a spatial TV constraint with
reordering. The ordering of the data was
obtained using the image reconstructed from fully sampled data.
Figure 5
Reordering method for 2D
images. (a) Simulated piecewise
constant heart image. (b) Image
reconstructed using IFT from ~15% of the full Fourier data, undersampled in a
variable density random fashion. (c) Image
reconstructed from undersampled data using a TV spatial constraint. (d) Actual MR magnitude image of the
short-axis slice of a heart at a single point in a perfusion sequence
reconstructed from fully sampled k-space data using IFT. (e) Corresponding IFT reconstruction from R~3 k-space data
undersampled in VD random fashion. (f) Reconstruction using a 2D TV constraint without any reordering. (g) Row-reordered image of the real
part of the complex MR image of the heart. (h) Reconstructed image with spatial reordering using a TV constraint. Ordering of
the data here was obtained using the image reconstructed from fully sampled data.
Figure 6 shows a plot comparing the
reconstruction error with increasing number of perturbations in the exact
spatial ordering for the actual MR heart image in Figure 5(d). The
reconstruction error is calculated as the total absolute difference between the
full data reconstruction and the data reconstructed using the TV spatial constraint.
A value of 10 on the X-axis means that the sorting-order vectors for 10% of the
total number of rows (rounded to nearest integer and randomly picked) and those
for 10% of the total number of columns (rounded to nearest integer and randomly
picked) are randomly perturbed for both the real and imaginary parts of the
complex image data.
Figure 6
Comparison of errors in the reconstruction for the actual MR heart
image in Figure 5(d) without reordering and with reordering as a function of
perturbations in the exact spatial ordering.
Perturbation for
a given row or a column is done independently for the entire length of the
sorting-order vector as described for the 1D case in Section 2.4. A value of
100 on the X-axis means that the sorting-order vectors for all the rows and all
the columns are completely perturbed (randomly and independently) for real and
imaginary parts of the image. The error for the reconstruction with reordering
is gradually increasing with increasing perturbations and when the exact
sorting orders are severely modified, the error gets higher than that without
reordering.
2.6. Reordering: multiple dimensions
The
reordering method described above can be extended to multi-image MR
acquisitions like dynamic myocardial perfusion imaging and brain DTI. In
perfusion imaging, a series of images of the heart are acquired to track the
uptake and washout patterns of the contrast agent in the myocardium. DTI
requires the acquisition of multiple images with diffusion weightings in different
directions. Reordering can be done in the multi-image dimension—in the time
dimension for the case of myocardial perfusion imaging and in the diffusion
encoding dimension for the case of DTI. As in the 1D case, reordering in the multi-image dimension for the
images can give a better reconstruction when the signal changes in the
dimension are not smoothly varying which is the case for perfusion imaging with
respiratory motion and for DTI. The
constraint for the reordering in the multi-image dimension is represented as where ∇ represents the gradient operator in the
multi-image dimension and is the data reordered in the corresponding
dimension. The subscript t is used
because the multi-image dimension is analogous to the temporal dimension of
dynamic perfusion datasets. For a given image frame in the multi-image dataset,
2D spatial reordering can also be included as described in Section 2.4.Reconstruction
can then be performed by using TV constraints in both space and multi-image
dimensions and with reordering in the corresponding dimensions
as follows: A similar
framework to (4) was proposed
in [12] for reconstructing undersampled radial
myocardial perfusion data but without reordering and with a different temporal
constraint. As in [12], (4)
will be referred to as a spatio-temporal constrained reconstruction (STCR).
3. APPLICATIONS
3.1. Dynamic phantom data
The reordering method for
multi-image acquisitions (4) was tested using a dynamic phantom. Gd was slowly
injected into a tube running through a water phantom and fully sampled
Cartesian k-space data were
acquired over time using an echoplanar imaging sequence on a Siemens 3T Trio
scanner. Raw k-space data was then undersampled offline in a variable density
(VD) pseudorandom fashion, in which 12 central low-resolution k-space lines
were sampled for all time frames, and the remaining phase encodes were sampled
in a pseudorandom fashion to give a net reduction factor of three. The acquisition
matrix for the scan was 256 × 72. Reconstruction from the undersampled data was then performed according
to (4) in two steps. In the first step,
the information about the reordering was obtained using images obtained using
the central low-resolution data from VD undersampling. The image
estimates were reordered first in the time dimension only and the
reconstruction was performed. In this step, the real and imaginary parts of the
complex low-resolution image space data for each pixel were sorted
independently in the time dimension according to their intensity values. The
corresponding sorting orders for the real and imaginary parts were used for
reordering the real and imaginary parts of the complex undersampled image space
data. After performing an initial reconstruction with only temporal reordering,
the resulting data were used to determine the spatial ordering. Final
reconstruction was then performed using spatial and temporal reordering.
Results of the final reconstruction with reordering were compared to full data
reconstructions using the standard inverse Fourier transform and to the
reconstructions without any reordering.
3.2. Dynamic myocardial perfusion and brain DTI data
The reordering method was applied
on dynamic myocardial perfusion imaging with respiratory motion and on brain
DTI data. Full Cartesian raw k-space perfusion data were obtained using a Siemens 3T Trio
scanner using a TurboFLASH saturation recovery sequence. The parameters for the
data acquisition were TR = 1.8 milliseconds, TE = 1 millisecond, flip angle = 12°, Gd dose = 0.025 mmol/kg, slice thickness = 6 mm, and
acquisition matrix = 192 × 96. FOV = 380 × 285 mm2. The data were acquired with
informed consent in accordance with the University of Utah Institutional Review Board. Brain DTI image data were
acquired on a GE 3T Scanner and full k-space data were generated from the magnitude image data by
applying 2D Fourier transforms on each diffusion encoding direction. Full
k-space data for both perfusion and brain DTI data were undersampled in a variable density
pseudorandom fashion outside the center and with the central 18 k-space lines
sampled for each time frame, and reconstruction was performed in two steps as
described in Section 3.1. The net R value for the perfusion data was 2.5 while
that for the DTI data was 3.
4. RESULTS
4.1. Dynamic phantom data
The
results of the reordering method on the multi-image phantom data are shown in
Figure 7. Figure 7(a) shows the image of a slice that was reconstructed from
full data using IFT at single time point. Figure 7(b) shows the corresponding
image reconstructed from R~3 data using STCR without any reordering. Figure 7(c)
shows the image reconstructed from R~3 data using STCR with reordering in both
temporal and spatial dimensions.
Figure 7
Results of multi-image
reordering method on dynamic phantom data. Image at a time point reconstructed (a) from full k-space data using IFT, (b) from R~3 data using STCR without any reordering, and (c) from R~3 data using STCR with
reordering in time and spatial dimensions. (d) Absolute difference image between Figures 7(a) and 7(b). (e) Absolute difference image between
Figures 7(a) and 7(c).
Figure 7(d)
shows the absolute difference image between Figures 7(a) and 7(b) and
Figure 7(e) shows the absolute difference image between Figures 7(a) and 7(c). The images in Figures 7(d) and 7(e) are scaled to the
same window level to highlight the differences. Figure 7(d) has more structure as compared to Figure 7(e).
4.2. Dynamic myocardial perfusion
The
results of the reordering method for dynamic myocardial perfusion imaging are
shown in Figure 8. Figure 8(a) (column) shows images at two different time
points in a perfusion sequence reconstructed from full perfusion data using
standard inverse Fourier transforms. Figure 8(b) (column) shows the
corresponding STCR reconstructions from R~2.5 data without any reordering
in time or space dimensions. Figure 8(c) (column) shows the corresponding STCR
reconstructions with reordering in both time and space dimensions.
Figure 8
Result of multi-image
reordering method on dynamic myocardial perfusion data. (a) Images at two different time points in the sequence
reconstructed from full k-space data (first column). (b) Corresponding images reconstructed from R~2.5 k-space data,
undersampled in variable density random fashion, using constrained
reconstruction method in (4) but without any reordering (second column). The
arrows point to the residual artifacts in the images. (c) Corresponding images reconstructed from R~2.5 k-space data
using constrained reconstruction method in (4) with reordering (third column).
The
reordering helps in reconstruction when there is a significant respiratory motion in the
data. We previously reported higher acceleration
factors (R~4 with interleaved undersampling and R~5 with variable density
sampling) in [3] for myocardial perfusion, when there was minimal or no
respiratory motion in the data. In the presence of significant respiratory
motion, the method in [3] was not fully able to resolve the artifacts from
undersampling. The current method was better able to reduce the artifacts even
in the presence of large respiratory motion.
4.3. Multi-image brain DTI data
The
results obtained by applying the reordering method on brain DTI data are shown
in Figure 9.
Figure 9
Result of the reordering
method on multi-image brain DTI data. (a) Image of a single diffusion encoding direction reconstructed from full Fourier
data. A line for comparison of pixel intensity profiles for different
reconstructions is also shown. (b) Corresponding encoding direction reconstructed from R~3 Fourier data,
undersampled in variable density random fashion, using constrained
reconstruction in (4) but without any reordering. (c) Corresponding direction reconstructed from the incomplete
Fourier data using constrained reconstruction in (4) with reordering. (d) Comparison of intensity line
profiles for images in Figures 9(a) and 9(b). (e) Comparison of intensity line profiles for images in Figures 9(a)
and 9(c).
Figure 9(c) matches Figure 9(a) better especially
around the ventricular regions. Figure 9(d) compares the line intensity
profiles for full data reconstruction (Figure 9(a)) and the reconstruction
without reordering (Figure 9(b)). Figure 9(e) compares the intensity profiles
for full data reconstruction (Figure 9(a)) and the reconstruction with
reordering (Figure 9(c)). The signals in Figure 9(e) match better than those in
Figure 9(d).
5. DISCUSSION
This
paper introduces a modified constraint term for compressed sampling and
constrained image reconstruction approaches. In general, it is possible to
choose a regularization or constraint term which is a good model for the image
being reconstructed. The basic idea of the reordering method is that it is
possible to tailor these regularization or constraint operators to improve the
reconstruction by reordering the signal. From a compressed sampling point of
view, various transforms have been proposed to enforce sparsity in the data.
Reordering can be thought as a new set of data-specific “transforms” that
further improve the sparsity. Recently, a new method using a prior image
constraint [17] was proposed to improve the constrained reconstruction of
dynamic CT images. The additional prior image constraint minimizes the L
1
distance between the estimated solution and the prior image. The reordering
method proposed here is different in the sense that it does not directly use
the intensities in the prior image. The method uses only the ordering
information from a prior image or set of images, which can be preserved if the
prior images are at a different and unknown intensity scale as compared to the
estimated solution.Reordering
can be done in multiple dimensions to improve the sparsity when the signals are
not smoothly varying. Here, we used images from the central low-resolution data
to determine orderings initially in the multi-image dimension and then used the
resulting images to obtain the spatial reordering for each image separately.
This is because the central low-resolution data are more faithful in the multi-image dimension
than they are in
the spatial dimension. Reordering in the multi-image dimension offered more
significant improvements as compared to reordering in the spatial dimensions.
This is because the temporal constraint generally plays a more important role
in resolving the artifacts as compared to the spatial constraint for dynamic
imaging [12]. To obtain significant improvements just using spatial reordering,
a good high-resolution reference image may be required. Improved ways of
obtaining reordering, like doing a separate training scan before the actual
acquisition, may help to achieve higher accelerations.The
reordering method incorporates the ordering information of the signal to better
match the total variation constraint assumption and thus improves the
reconstruction from undersampled data. Methods like adaptive regularization
[18, 19] were proposed to improve the performance of TV regularization-based denoising
techniques by using a priori
information about the signal. In these methods, the regularization parameter is
varied based on the a priori
knowledge of the locations of edges and smooth regions in a signal, so that
less regularization is done where strong edges are present in the signal. While
this type of approach may be extended to TV constrained reconstruction,
choosing the optimal amount of variation of the regularization parameter can be
complicated for rapidly varying signals. An alternative method that can use
such a priori information was explored here with the reordering method that
uses only a single regularization parameter.The
reordering method may not be appropriate when the ordering is incorrect in such
a way that the total variation of the reordered full image sets is increased as
compared to that of the original full data. In practice, it might not be
possible to know this information beforehand. In such cases, L-curves can be
used to determine to some extent if reordering is appropriate. L-curves can be
computed for reconstructions with and without reordering and the TV norms
corresponding to the optimal regularization parameters can be compared. If the
ordering is appropriate, then the TV norm corresponding to the optimal
regularization parameter with reordering is lower than that for the
corresponding optimal regularization parameter without reordering. Consider
Figure 10(a) which shows the L-curve obtained for the 1D randomly varying curve
shown in Figure 1(b), with a large number of random perturbations (~65%) in the
exact ordering. The TV norm corresponding to the optimal α is 36.08. When the number of random perturbations is decreased (~21%), the L-curve
in Figure 10(b) is obtained and the TV norm corresponding to the optimal α is 5.02. The L-curve in Figure 10(a) is
overlaid in Figure 10(b) for reference. The TV norm corresponding to the
L-curve obtained without reordering is 14.05.
Figure 10
(a) L-curve obtained for reconstruction of the nonsmooth signal in
Figure 1(b) from R~2 Fourier data with reordering, but with large number (~65%)
of random perturbations in the exact ordering. (b) L-curve obtained for reconstruction of the nonsmooth signal in
Figure 1(b) from R~2 Fourier data with reordering with fewer (~21%) random
perturbations in the exact ordering. The L-curve in Figure 10(a) is also
overlaid.
The
reconstruction time with image reordering was higher than the standard L
1
norm
reconstruction, as in each iteration, the estimated signal is reordered before
computing the constraint update. For the data reordering in 1D case, the
reconstruction time was 1.04 times slower, while that for the dynamic case with
reordering in both spatial and temporal dimensions was 2.8 times slower. It took ~35 seconds
per iteration on a linux machine with an AMD processor (2.5 Ghz) and 6 GB ram
for STCR with reordering in multiple dimensions. The implementation was done in
MATLAB and a host of methods including the use of GPUs are available to greatly
speed up reconstruction methods.
6. CONCLUSION
A
method involving reordering in time and space dimensions of the image estimates
to better match the chosen constraints of an inverse problem-type
reconstruction was presented. The method uses non-reordered reconstructions to
obtain information about the signal to be reconstructed to determine the
orderings of the pixel intensities. The orderings can be estimated from the low-resolution
images when a variable density undersampling scheme is used, and from
non-reordered constrained reconstructions. The method can be forgiving to errors
in the images used to choose the orderings as the method does not use the data
directly but uses only its ordering information. The method was shown to have
promise for cardiac perfusion imaging and offered some small improvements for
DTI data. Future improvements in finding more optimal reorderings, perhaps as
part of the estimation process, may make the approach useful in a wide array of
applications.
Authors: R Van de Walle; H H Barrett; K J Myers; M I Altbach; B Desplanques; A F Gmitro; J Cornelis; I Lemahieu Journal: IEEE Trans Med Imaging Date: 2000-12 Impact factor: 10.048
Authors: Ganesh Adluru; Yaniv Gur; Liyong Chen; David Feinberg; Jeffrey Anderson; Edward V R DiBella Journal: Med Phys Date: 2015-08 Impact factor: 4.071
Authors: Saiprasad Ravishankar; Brian E Moore; Raj Rao Nadakuditi; Jeffrey A Fessler Journal: IEEE Trans Med Imaging Date: 2017-01-10 Impact factor: 10.048
Authors: Li Feng; Leon Axel; Hersh Chandarana; Kai Tobias Block; Daniel K Sodickson; Ricardo Otazo Journal: Magn Reson Med Date: 2015-03-25 Impact factor: 4.668
Authors: Li Feng; Monvadi B Srichai; Ruth P Lim; Alexis Harrison; Wilson King; Ganesh Adluru; Edward V R Dibella; Daniel K Sodickson; Ricardo Otazo; Daniel Kim Journal: Magn Reson Med Date: 2012-08-06 Impact factor: 4.668
Authors: Anil K Attili; Andreas Schuster; Eike Nagel; Johan H C Reiber; Rob J van der Geest Journal: Int J Cardiovasc Imaging Date: 2010-02 Impact factor: 2.357